The Forsyth Institute, Center for Clinical and Translational Research (CCTR), Cambridge, Massachusetts, USA.
Department of Basic and Translational Sciences, University of Pennsylvania, Penn Dental Medicine, Philadelphia, Pennsylvania, USA.
J Clin Invest. 2021 Dec 1;131(23). doi: 10.1172/JCI152973.
BackgroundGingivitis and periodontitis are prevalent inflammatory diseases of the periodontal tissues. Current treatments are often ineffective or do not prevent disease recurrence. Uncontrolled complement activation and the resulting chronic gingival inflammation are hallmarks of periodontal diseases. We determined the efficacy and safety of a complement 3-targeted therapeutic, AMY-101, which was locally administered to adult patients with periodontal inflammation.MethodsThirty-two patients with gingival inflammation were enrolled in a randomized, placebo-controlled, double-blind, split-mouth phase IIa trial that followed a dose escalation study to select a safe and effective dose in an additional 8 patients. Half of the patient's mouth was randomly assigned to AMY-101 (0.1 mg/site) or placebo injections at sites of inflammation, administered on days 0, 7, and 14, and then evaluated for safety and efficacy outcomes on days 28, 60, and 90. The primary efficacy outcome was a change in gingival inflammation, measured by a modified gingival index (MGI), and secondary outcomes included changes in bleeding on probing (BOP), the amount of plaque, pocket depth, clinical attachment level, and gingival crevicular fluid levels of matrix metalloproteinases (MMPs) over 90 days.ResultsA once-weekly intragingival injection of AMY-101 for 3 weeks was safe and well tolerated in all participants and resulted in significant (P < 0.001) reductions in clinical indices measuring gingival inflammation (MGI and BOP). AMY-101 significantly (P < 0.05) reduced MMP-8 and MMP-9 levels, indicators of inflammatory tissue destruction. These therapeutic effects persisted for at least 3 months after treatment.ConclusionAMY-101 treatment resulted in a significant and sustainable reduction in gingival inflammation without adverse events and, we believe, merits further investigation for the treatment of periodontitis and other oral or peri-implant inflammatory conditions.Trial registrationClinicalTrials.gov identifier NCT03694444.FundingAmyndas Pharmaceuticals.
牙龈炎和牙周炎是牙周组织常见的炎症性疾病。目前的治疗方法往往效果不佳或不能预防疾病复发。补体失控激活和由此导致的慢性牙龈炎症是牙周病的标志。我们确定了一种补体 3 靶向治疗药物 AMY-101 的疗效和安全性,该药物局部应用于患有牙周炎症的成年患者。
32 名患有牙龈炎症的患者参加了一项随机、安慰剂对照、双盲、分侧的 2a 期临床试验,该试验在另外 8 名患者中进行了剂量递增研究,以选择安全有效的剂量。患者口腔的一半被随机分配到 AMY-101(0.1mg/部位)或安慰剂注射部位的炎症,在第 0、7 和 14 天给药,然后在第 28、60 和 90 天评估安全性和疗效结果。主要疗效终点是改良牙龈指数(MGI)测量的牙龈炎症变化,次要终点包括探诊出血(BOP)、菌斑量、牙周袋深度、临床附着水平和牙龈沟液中基质金属蛋白酶(MMPs)的变化。
每周一次的 AMY-101 龈内注射治疗 3 周,所有参与者均安全耐受,临床指标测量的牙龈炎症(MGI 和 BOP)显著降低(P <0.001)。AMY-101 显著(P <0.05)降低了 MMP-8 和 MMP-9 水平,这是炎症性组织破坏的指标。这些治疗效果在治疗后至少 3 个月内持续存在。
AMY-101 治疗可显著且持续降低牙龈炎症,无不良反应,我们认为,值得进一步研究用于治疗牙周炎和其他口腔或种植体周围炎症性疾病。
ClinicalTrials.gov 标识符 NCT03694444。
Amyndas 制药公司。